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Hemoglobin
international journal for hemoglobin research
Volume 24, 2000 - Issue 3
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Original Article

Very Mild Pathology in a Case of Hb S/β˚-Thalassemia in Combination with a Homozygosity for the α-Thalassemia 3.7 kb Deletion

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Pages 259-263 | Received 03 Mar 2000, Accepted 12 Apr 2000, Published online: 07 Jul 2009

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Maryam Neishabury, Christian Oberkanins, Lia Abbasi Moheb, Ali Akbar Pourfathollah, Kimia Kahrizi, Elahe Keyhany, Walter Krugluger & Hossein Najmabadi. (2003) High Prevalence of the −α3.7 Deletion Among Thalassemia Patients in Iran. Hemoglobin 27:1, pages 53-55.
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P. C. Giordano, W. Huisman & C. L. Harteveld. (2011) Iron Depletion: An Ameliorating Factor for Sickle Cell Disease?. ISRN Hematology 2011, pages 1-4.
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Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallMartin H. Steinberg. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 564 586 .
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallMartin H. Steinberg. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 435 436 .
Karen E Papez & William E Smoyer. (2004) Recent advances in congenital nephrotic syndrome. Current Opinion in Pediatrics 16:2, pages 165-170.
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